Diverse driving forces underlie the invariant occurrence of the T42A, E139D, I282V and T468M SHP2 amino acid substitutions causing Noonan and LEOPARD syndromes (Q33979110)
Jump to navigation
Jump to search
scientific article
Language | Label | Description | Also known as |
---|---|---|---|
English | Diverse driving forces underlie the invariant occurrence of the T42A, E139D, I282V and T468M SHP2 amino acid substitutions causing Noonan and LEOPARD syndromes |
scientific article |
Statements
1 reference
Diverse driving forces underlie the invariant occurrence of the T42A, E139D, I282V and T468M SHP2 amino acid substitutions causing Noonan and LEOPARD syndromes (English)
1 reference
1 reference
Gianni Cesareni
1 reference
Simone Martinelli
1 reference
Michele Tinti
1 reference
Elisabetta Flex
1 reference
Marina Ceccarini
1 reference
Antonio Palleschi
1 reference
Tamara C Petrucci
1 reference
27 March 2008
1 reference
1 reference
17
1 reference
13
1 reference
2018-2029
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
Identifiers
1 reference
1 reference
1 reference